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Maintenance of Primary Hepatocyte Functions In Vitro by Inhibiting Mechanical Tension-Induced YAP Activation

Authors :
Pingxin Sun
Guanyu Zhang
Xiaohui Su
Caixia Jin
Bing Yu
Xinlu Yu
Zhuman Lv
Haoxin Ma
Mingliang Zhang
Wanguo Wei
Wenlin Li
Source :
Cell Reports, Vol 29, Iss 10, Pp 3212-3222.e4 (2019)
Publication Year :
2019
Publisher :
Elsevier, 2019.

Abstract

Summary: Hepatocytes are the primary functional cells of the liver, performing its metabolic, detoxification, and endocrine functions. Functional hepatocytes are extremely valuable in drug discovery and evaluation, as well as in cell therapy for liver diseases. However, it has been a long-standing challenge to maintain the functions of hepatocytes in vitro. Even freshly isolated hepatocytes lose essential functions after short-term culture for reasons that are still not well understood. In the present study, we find that mechanical tension-induced yes-associated protein activation triggers hepatocyte dedifferentiation. Alleviation of mechanical tension by confining cell spreading is sufficient to inhibit hepatocyte dedifferentiation. Based on this finding, we identify a small molecular cocktail through reiterative chemical screening that can maintain hepatocyte functions over the long term and in vivo repopulation capacity by targeting actin polymerization and actomyosin contraction. Our work reveals the mechanisms underlying hepatocyte dedifferentiation and establishes feasible approaches to maintain hepatocyte functions. : It has been a long-standing challenge to maintain the functions of hepatocytes in vitro. Sun et al. find that mechanical tension-induced Yap activation triggers hepatocyte dedifferentiation. Alleviation of mechanical tension by confining cell spreading or treatment with a small molecule cocktail targeting actin/actomyosin dynamics could maintain hepatocyte functions. Keywords: hepatocytes, dedifferentiation, small molecules, mechanical tension

Subjects

Subjects :
Biology (General)
QH301-705.5

Details

Language :
English
ISSN :
22111247
Volume :
29
Issue :
10
Database :
Directory of Open Access Journals
Journal :
Cell Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.34775e07111a4c6cb1a99539edcf0e52
Document Type :
article
Full Text :
https://doi.org/10.1016/j.celrep.2019.10.128